Campos-Martorell Mireia, Cano-Sarabia Mary, Simats Alba, Hernández-Guillamon Mar, Rosell Anna, Maspoch Daniel, Montaner Joan
Neurovascular Research Laboratory, Institut de Recerca Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona.
Catalan Institute of Nanoscience and Nanotechnology (ICN2), CSIC and The Barcelona Institute of Science and Technology, Universitat Autònoma de Barcelona, Barcelona.
Int J Nanomedicine. 2016 Jun 29;11:3035-48. doi: 10.2147/IJN.S107292. eCollection 2016.
Although the beneficial effects of statins on stroke have been widely demonstrated both in experimental studies and in clinical trials, the aim of this study is to prepare and characterize a new liposomal delivery system that encapsulates simvastatin to improve its delivery into the brain.
In order to select the optimal liposome lipid composition with the highest capacity to reach the brain, male Wistar rats were submitted to sham or transitory middle cerebral arterial occlusion (MCAOt) surgery and treated (intravenous [IV]) with fluorescent-labeled liposomes with different net surface charges. Ninety minutes after the administration of liposomes, the brain, blood, liver, lungs, spleen, and kidneys were evaluated ex vivo using the Xenogen IVIS(®) Spectrum imaging system to detect the load of fluorescent liposomes. In a second substudy, simvastatin was assessed upon reaching the brain, comparing free and encapsulated simvastatin (IV) administration. For this purpose, simvastatin levels in brain homogenates from sham or MCAOt rats at 2 hours or 4 hours after receiving the treatment were detected through ultra-high-protein liquid chromatography.
Whereas positively charged liposomes were not detected in brain or plasma 90 minutes after their administration, neutral and negatively charged liposomes were able to reach the brain and accumulate specifically in the infarcted area. Moreover, neutral liposomes exhibited higher bioavailability in plasma 4 hours after being administered. The detection of simvastatin by ultra-high-protein liquid chromatography confirmed its ability to cross the blood-brain barrier, when administered either as a free drug or encapsulated into liposomes.
This study confirms that liposome charge is critical to promote its accumulation in the brain infarct after MCAOt. Furthermore, simvastatin can be delivered after being encapsulated. Thus, simvastatin encapsulation might be a promising strategy to ensure that the drug reaches the brain, while increasing its bioavailability and reducing possible side effects.
尽管他汀类药物对中风的有益作用已在实验研究和临床试验中得到广泛证实,但本研究的目的是制备并表征一种新的脂质体递送系统,该系统包裹辛伐他汀以改善其向脑内的递送。
为了选择能够最大程度到达脑内的最佳脂质体脂质组成,将雄性Wistar大鼠进行假手术或短暂性大脑中动脉闭塞(MCAOt)手术,并静脉注射具有不同净表面电荷的荧光标记脂质体进行治疗。脂质体给药90分钟后,使用Xenogen IVIS(®) Spectrum成像系统对脑、血液、肝脏、肺、脾脏和肾脏进行离体评估,以检测荧光脂质体的负载情况。在第二项子研究中,比较了游离辛伐他汀和包裹型辛伐他汀静脉给药后在脑内的情况。为此,通过超高效液相色谱法检测接受治疗后2小时或4小时假手术或MCAOt大鼠脑匀浆中的辛伐他汀水平。
带正电荷的脂质体在给药90分钟后未在脑或血浆中检测到,而中性和带负电荷的脂质体能够到达脑内并特异性地积聚在梗死区域。此外,中性脂质体在给药4小时后在血浆中表现出更高的生物利用度。超高效液相色谱法对辛伐他汀的检测证实,无论是作为游离药物还是包裹在脂质体中给药,它都能够穿过血脑屏障。
本研究证实脂质体电荷对于促进其在MCAOt后脑梗死中的积聚至关重要。此外,辛伐他汀可以在包裹后递送。因此,辛伐他汀包裹可能是一种有前景的策略,可确保药物到达脑内,同时提高其生物利用度并减少可能的副作用。